Mattia Camera
Overview
Explore the profile of Mattia Camera including associated specialties, affiliations and a list of published articles.
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Articles
5
Citations
11
Followers
0
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Recent Articles
1.
Massucco S, Fossa P, Fiorillo C, Faedo E, Gemelli C, Barresi R, et al.
Front Genet
. 2024 Dec;
15:1437859.
PMID: 39703226
Recessively inherited limb-girdle muscular dystrophy type 1, caused by mutations in the calpain 3 gene, is the most common limb-girdle muscular dystrophy worldwide. Recently, cases of autosomal dominant calpainopathy have...
2.
Capodivento G, Camera M, Liessi N, Trada A, Debellis D, Schenone A, et al.
Int J Mol Sci
. 2024 Oct;
25(20).
PMID: 39457026
Findings accumulated over time show that neurophysiological, neuropathological, and molecular alterations are present in CMT1A and support the dysmyelinating rather than demyelinating nature of this neuropathy. Moreover, uniform slowing of...
3.
Liaci C, Camera M, Zamboni V, Saro G, Ammoni A, Parmigiani E, et al.
Front Cell Dev Biol
. 2022 Dec;
10:875468.
PMID: 36568982
GTPases of the Rho family are components of signaling pathways linking extracellular signals to the control of cytoskeleton dynamics. Among these, RAC1 plays key roles during brain development, ranging from...
4.
Camera M, Russo I, Zamboni V, Ammoni A, Rando S, Morellato A, et al.
Front Neurosci
. 2022 Mar;
16:744693.
PMID: 35237119
p140Cap, encoded by the gene (, is an adaptor/scaffold protein highly expressed in the mouse brain, participating in several pre- and post-synaptic mechanisms. knock-out (KO) female mice show severe hypofertility,...
5.
Liaci C, Camera M, Caslini G, Rando S, Contino S, Romano V, et al.
Int J Mol Sci
. 2021 Jul;
22(11).
PMID: 34200511
Intellectual disability (ID) is a pathological condition characterized by limited intellectual functioning and adaptive behaviors. It affects 1-3% of the worldwide population, and no pharmacological therapies are currently available. More...